Thalassemia Treatment Cost In India
Thalassemias are a group of inherited blood diseases that affect the production of hemoglobin (the protein responsible for transporting oxygen). They are of varying severity: some cause no symptoms while others are life-threatening. A bone marrow transplant is considered in the most serious cases for thalassemia treatment.
What Is Thalassemia?
Thalassemia is characterized by a defect in the production of hemoglobin. As a reminder, hemoglobin is a large protein found in red blood cells (red cells) whose role is to ensure the transport of dioxygen from the respiratory system to the rest of the body.
It is said that Thalassemia is a blood disease. The transport function of red blood cells is impaired, which can have serious consequences for the body. At this stage, it happens to be significant to note that several types of Thalassemia have neither the same characteristics nor the same degree of severity. Some cause no symptoms, while others are life-threatening.
WHAT CAUSES THALASSEMIA?
Thalassemias are genetic diseases. They are due to the alteration of one or more genes involved in the synthesis of hemoglobin, and more precisely, to the alteration of the genes involved in the production of the protein chains of hemoglobin. There are four of these: two alpha chains and two beta chains.
Each of these chains can be affected in the event of Thalassemia. There are also:
- Alpha thalassemias are characterized by an alteration of the alpha chain;
- Beta thalassemias are characterized by an alteration of the beta chain.
The severity of alpha thalassemia and beta-thalassemia major treatment depends on the number of altered genes. The more important it is, the higher the degree of severity.
A blood test makes the diagnosis of Thalassemia. The blood count makes it possible to evaluate the appearance and the number of red blood cells, and thus to know the total amount of hemoglobin. Biochemical analysis of hemoglobin makes it possible to distinguish alpha-thalassemia from beta-thalassemia. Finally, genetic analyzes make it possible to assess the number of altered genes and thus to define the severity of Thalassemia.
Symptoms Of Thalassemia
The symptoms of Thalassemia are very variable depending on the case and mainly depend on the degree of alteration of the genes involved in the production of the protein chains of hemoglobin. Thalassemias may cause no symptoms in their minor forms and be life-threatening in their most severe forms.
The symptoms mentioned below only concern the intermediate to major forms of Thalassemia. These are just the main symptoms. Very specific symptoms can sometimes be seen depending on the type of Thalassemia.
Thalassemia Treatment Cost In India
Starting USD 20,000
( Indian Rupees Approx. 14,40,000 )
The typical sign of Thalassemia is anemia. It is a lack of hemoglobin that can result in the appearance of different symptoms:
- Shortness of breath
The strength of these symptoms differs based on the rigorousness of the Thalassemia.
- People with Thalassemia may have jaundice (jaundice) visible in the skin or the whites of the eyes.
Stone formation inside the gallbladder can also be seen. The calculations are sort of “little pebbles.”
It is an upsurge in the size of the spleen. One of the roles of this organ is to filter the blood and filter out harmful substances, including abnormal red blood cells. In the event of Thalassemia, the spleen is strongly mobilized and gradually increases in size. Pain may be felt.
Other Rarer Symptoms
More rarely, severe forms of Thalassemia can lead to other abnormalities. It can, for example, be observed:
- Hepatomegaly that is, an increase in the size of the liver;
- Bone deformities;
- Delayed development of the child
The management of Thalassemia is essential to limit the occurrence of these complications.
The management of Thalassemia depends on many parameters, including the type of Thalassemia, its severity, and the condition of the person concerned. The minor forms do not require treatment, while the severe forms require very regular medical monitoring.
The treatments mentioned below only concern the intermediate to major forms of Thalassemia.
Correction of Anemia
When the lack of hemoglobin is too great, regular blood transfusions are necessary. They consist of injecting the person concerned with blood or red blood cells taken from a donor to maintain an acceptable level of red blood cells in the blood.
Vitamin B9 supplementation
It may be recommended to start a daily vitamin B9 supplement because the needs for this vitamin are increased in the event of Thalassemia. Vitamin B9 is involved in the production of red blood cells.
A splenectomy is the surgical removal of the spleen. This operation can be considered when anemia is very important.
Treatment of iron overload
Thalassemic people have an iron overload in their bodies. This accumulation can lead to different complications. This is why iron chelators are proposed to remove excess iron.
Bone marrow transplant
This is the only treatment that can cure Thalassemia permanently. It is a heavy treatment that is only offered in the most severe forms of the disease.
When should you consult a doctor?
Have an appointment with your doctor for an assessment if you have any of the signs or symptoms of Thalassemia.
Silent carrier and alpha thalassemia trait
The silent carrier and alpha thalassemia trait are not diseases and will not cause illness to your child in any way. Individuals with silent carriers and alpha thalassemia traits are not expected to have fatigue, low energy, or lack of vigor.
Get to Know about the factors Responsible for the Thalassemia Treatment in India:
Below mentioned are a few of the fundamental factors affecting the concerning the cost treatment of Thalassemia in India :
- Hospital standard and the quality of the doctor, and overall medical procedures
- Consultation fees of the doctors
- Diagnostic procedures rate
- Surgery cost involved
- Cost involves in other therapies related to Thalassemia
Reach out to our experts for the best and affordable Thalassemia Treatment Cost in India.
The Most Important Frequently Asked Questions
Q: Can you tell me the rough estimate of the price for the treatment of Thalassemia in India?
A: Expect the price for thalassemia treatment in India to be a litter higher because it involves a bone marrow transplant. But if you are an international tourist coming for the treatment from overseas, then you will get the good value of your dollars or euro. Your cost treatment would be starting @ 22000 USD and extends up to 25000 USD.
Q: What are the factors affecting the cost of the treatment?
A: From the standard of the hospital to the team of the doctors you select, the treatment cost depends upon the package you select, the number of travelers you are coming to India, and for how many days you would have to stay in India for the treatment.
Q: Who to consult for the thalassemia treatment?
A: Consult a hematologist, or you could visit the general physician. On the flip side, there are cases when one must have to examine themselves under the supervision of a cardiologist, endocrinologist, and even gastroenterologists too!
Q: What if a person is suffering from Thalassemia? Can he lead a normal life?
A: Of course, you can do that too, with normal life survival. But if you have a condition where your heart is affected due to beta-thalassemia, the condition may turn worse. So, it’s advisable to consult the physician.
Q: Is thalassemia disease passed on by parents to their kids?
A: YES! Thalassemia is an intrinsic disease, and it could pass onto your children too. So, consult a dedicated specialist.
Q: What is a thalassemia bearer?
A: Patients experiencing Thalassemia do convey Thalassemia but generally don’t encounter any recognized medical issues except iron deficiency. Contingent on the absence of the type of whichever beta-protein, the patient may have either alpha thalassemia or beta-thalassemia.
Q: Should I consider thalassemia disease lethal?
A: Well, if you have thalassemia minor, then it’s not a death-dealing. But if you have thalassemia major, your chances of survival decrease if you don’t undergo proficient medical treatment.
Q: How curable Thalassemia is?
A: Patients with extreme Thalassemia rely upon blood transfusions. A bone marrow transplant can be beneficial to fix Thalassemia, but the greater part of the occasions, it gets difficult to discover compatible donors.
Q: How is the common Thalassemia?
A: If we talk about worldwide statistics, beta-thalassemia is widely common. Every ear, thousands of infants are born with this disorder or disease.
Q: When is the ideal time to go for the testing of Thalassemia?
A: You must go to the doctor and consult if you are planning for a baby or your wife or you are at the initial stage of pregnancy.
Q: Are there any specific documents I need to carry during my medical treatment to India?
A: YES! Bookmark your copy of the medical file from the concerned doctor or hostile in India, which includes the patient’s information or hospital information. Also, blood tests, other health problems, prescriptions, and contact of the hospital or doctor is concerned, and you must carry those documents too!
Q: Does India offer a visa on arrival for the treatment?
A: Congrats yourself and consider yourself lucky if you are a citizen of the following countries – Japan, Cambodia, Finland, Indonesia, Philippines, Luxembourg, Myanmar, New Zealand, Singapore, South Korea and Vietnam, Bhutan, Nepal, and the Maldives can come to India for the treatment without the hassle of the visa problem up to 90 days!
Q: What are the requisite essentials for a clinical visa to India?
A: Keep a substantial identification like a Passport and visa and the proof of medical treatment papers of the hospitals in India. You can apply for a medical visa to India. Up to 2 specialists who are blood family members can go with the patient under orderly independent visas.
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